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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296598Generated: October 30, 2026

5,6-Diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil → HCID 178456519, compound

https://huagongshe.com/reaction/1296598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6-Diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracilHCID 11609665—
ReactantHCID 178525261HCID 178525261—
ProductHCID 178456519HCID 178456519—

Reaction Steps

By the method of Example 2, 1H-tetrazole-5-acetic acid is reacted with 5,6-diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil (6) to yield 3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine. By the method of Example 3, this substance is alkylated with a mixture of 1,2-dichloroethane, sodium carbonate, and ethylamine to yield 7-(2-ethylamino)ethyl-3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine. By the method of Example 4,7-(2-ethylamino)ethyl-3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine is reduced with hydrazine hydrate or hydrogen gas in the presence of a palladium catalyst to yield 3-[2-(4-aminophenyl)ethyl]-7-(2-ethylamino)ethyl-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine free base. The corresponding hydrochloride salt is then made on exposure to an excess of hydrogen chloride in solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247639B2
Source datasetuspto-grants-2007_07
ORD IDord-6b761e28d56f4c62ac4f26ccdd9c4751
Source noteuspto-grants-2007_07